Search results for "Imprinting"

showing 10 items of 124 documents

Trace analysis by ion mobility spectrometry: From conventional to smart sample preconcentration methods. A review.

2018

Ion mobility spectrometry (IMS) is a rapid and high sensitive technique widely used in security and forensic areas. However, a lack of selectivity is usually observed in the analysis of complex samples due to the scarce resolution of the technique. The literature concerning the use of conventional and novel smart materials in the pretreatment and preconcentration of samples previous to IMS determinations has been critically reviewed. The most relevant strategies to enhance selectivity and sensitivity of IMS determinations have been widely discussed, based in the use of smart materials, as immunosorbents, aptamers, molecularly imprinted polymers (MIPs), ionic liquids (ILs) and nanomaterial. …

Resolution (mass spectrometry)Ion-mobility spectrometryPolymersAptamerAnalytic Sample Preparation MethodsIonic LiquidsNanotechnology02 engineering and technologySmart material01 natural sciencesBiochemistryAnalytical ChemistryMolecular ImprintingIon Mobility SpectrometryEnvironmental ChemistrySpectroscopyChemistry010401 analytical chemistryMolecularly imprinted polymerAnalytic Sample Preparation MethodsImmunosorbentsAptamers Nucleotide021001 nanoscience & nanotechnology0104 chemical sciencesNanostructures0210 nano-technologyMolecular imprintingImmunosorbentsAnalytica chimica acta
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The mRNA degradation factor Xrn1 regulates transcription elongation in parallel to Ccr4

2019

Abstract Co-transcriptional imprinting of mRNA by Rpb4 and Rpb7 subunits of RNA polymerase II (RNAPII) and by the Ccr4–Not complex conditions its post-transcriptional fate. In turn, mRNA degradation factors like Xrn1 are able to influence RNAPII-dependent transcription, making a feedback loop that contributes to mRNA homeostasis. In this work, we have used repressible yeast GAL genes to perform accurate measurements of transcription and mRNA degradation in a set of mutants. This genetic analysis uncovered a link from mRNA decay to transcription elongation. We combined this experimental approach with computational multi-agent modelling and tested different possibilities of Xrn1 and Ccr4 acti…

Ribosomal ProteinsSaccharomyces cerevisiae ProteinsRNA StabilitymRNAMutantRNA polymerase IISaccharomyces cerevisiaeBiology03 medical and health sciencesGenomic Imprinting0302 clinical medicineRibonucleasesRibosomal proteinTranscription (biology)Gene Expression Regulation FungalGeneticsGenomesGene030304 developmental biologyRegulation of gene expression0303 health sciencesMessenger RNAGene regulation Chromatin and EpigeneticsFungal geneticsCell biologyExoribonucleasesbiology.proteinRNARNA Polymerase IIGenome FungalTranscriptional Elongation Factors030217 neurology & neurosurgery
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Rpb4 and Puf3 imprint and post-transcriptionally control the stability of a common set of mRNAs in yeast

2020

ABSTRACTGene expression involving RNA polymerase II is regulated by the concerted interplay between mRNA synthesis and degradation, crosstalk in which mRNA decay machinery and transcription machinery respectively impact transcription and mRNA stability. Rpb4, and likely dimer Rpb4/7, seem the central components of the RNA pol II governing these processes. In this work we unravel the molecular mechanisms participated by Rpb4 that mediate the posttranscriptional events regulating mRNA imprinting and stability. By RIP-Seq, we analyzed genome-wide the association of Rpb4 with mRNAs and demonstrated that it targeted a large population of more than 1400 transcripts. A group of these mRNAs was als…

Saccharomyces cerevisiae ProteinsTranscription GeneticRNA StabilityRNA polymerase IIRNA-binding proteinSaccharomyces cerevisiaeGenomic Imprinting03 medical and health sciences0302 clinical medicineTranscription (biology)Gene Expression Regulation FungalGene expressionRNA MessengerRNA Processing Post-TranscriptionalImprinting (psychology)Molecular Biology030304 developmental biology0303 health sciencesMessenger RNABinding SitesbiologyChemistryRNA-Binding ProteinsMolecular Sequence AnnotationCell BiologyChromatinChromatinCell biologyCrosstalk (biology)030220 oncology & carcinogenesisbiology.proteinRNA Polymerase IIProtein BindingResearch PaperRNA Biology
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Reliability and Fabrication of Molds for Nanoimprinting

2010

During the last decade there has been a growing attention to nanoscaled materials and to the related technologies to produce them. The problems to overcome in the manufacturing of these kinds of items increase dramatically on decreasing the dimension of the devices. In this sense, the scientific research has been strongly stimulated to try to improve and optimize all the critical issues. One of the most attractive fields in nanomanufacturing is related to nanoimprinting, i.e. to the possibility to transfer a nanoscaled pattern from a mold to another substrate. In this technology, among the others, there are two main critical steps: the preparation of a good mold and the use of a correct rel…

Settore ING-IND/22 - Scienza E Tecnologia Dei MaterialiFabricationMaterials scienceMold fabrication Nanoimprinting NanoLithography Nanomolds Nanopatterns Reliability ResistBiomedical EngineeringPharmaceutical ScienceMedicine (miscellaneous)BioengineeringReliability (statistics)BiotechnologyReliability engineeringCurrent Nanoscience
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Congenital malformations.

2012

Congenital malformations are single or multiple defects of the morphogenesis of organs or body districts identifiable at birth or during the intrauterine life. Their global birth prevalence is about 2–3%. Both genetic and environmental factors, as well as their combination in a multifactorial contest, may induce congenital defects. Congenital malformations may be classi- fied on the basis of clinical, etiologic as well as pathogenetic criteria. Relevant diagnostic and therapeutic tools have been progressively improving in the last decades, contributing to a better identification and a reduction of long-term morbidity and mortality of these patients. A correct identification of a congen- ita…

Settore MED/38 - Pediatria Generale E SpecialisticaPrenatal DiagnosisPediatrics Perinatology and Child HealthObstetrics and GynecologyDysostosesHumansassociation blastogenesis chromosome counseling gene imprinting methylation phenotype sequence syndrome uniparental dysomyGenetic CounselingSyndromeOsteochondrodysplasiasCongenital AbnormalitiesThe journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
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A Biocatalytic Nanomaterial for the Label-Free Detection of Virus-Like Particles

2017

International audience; The design of nanomaterials that are capable of specific and sensitive biomolecular recognition is an on-going challenge in the chemical and biochemical sciences. A number of sophisticated artificial systems have been designed to specifically recognize a variety of targets. However, methods based on natural biomolecular detection systems using antibodies are often superior. Besides greater affinity and selectivity, antibodies can be easily coupled to enzymatic systems that act as signal amplifiers, thus permitting impressively low detection limits. The possibility to translate this concept to artificial recognition systems remains limited due to design incompatibilit…

Silica mineralizationBiosilicificationNanoparticleNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryNanomaterialsMolecular ImprintingSilica nanoparticlesMolecular recognitionArtificial systems[SDV.IDA]Life Sciences [q-bio]/Food engineeringOrganosilicaMolecular BiologyLabel freeDetection limitChemistryOrganic ChemistryVirion[ SDV.IDA ] Life Sciences [q-bio]/Food engineering021001 nanoscience & nanotechnologyNanostructures0104 chemical sciencesVirusesBiocatalysisMolecular MedicineNanoparticlesMechanismMolecular recognition0210 nano-technologyMolecular imprinting
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Development of an improved method for trace analysis of quinolones in eggs of laying hens and wildlife species using molecularly imprinted polymers.

2012

A sensitive, selective, and efficient method was developed for simultaneous determination of 11 fluoroquinolones (FQs), ciprofloxacin, danofloxacin, difloxacin, enrofloxacin, flumequine, marbofloxacin, norfloxacin, ofloxacin, oxolinic acid, pipemidic acid, and sarafloxacin, in eggs by molecularly imprinted polymer (MIP) and column liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS). Samples were diluted with 50 mM sodium dihydrogen phosphate at pH 7.4, followed by purification with a commercial MIP (SupelMIP SPE-Fluoroquinolones). Recoveries for the 11 quinolones were in the range of 90-106% with intra- and interday relative standard deviation ranging from …

Spectrometry Mass Electrospray IonizationDanofloxacinPolymersanimal diseasesEggsImproved methodAnimals WildBiologyQuinolonesMolecular ImprintingLimit of DetectionmedicineEnrofloxacinAnimalsDifloxacinChromatographyMolecularly imprinted polymerGeneral Chemistrybiochemical phenomena metabolism and nutritionCiprofloxacinFlumequineTrace analysisFemaleGeneral Agricultural and Biological SciencesChickensmedicine.drugChromatography LiquidJournal of agricultural and food chemistry
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ADHD and DAT1: Further evidence of paternal over-transmission of risk alleles and haplotype

2010

Contains fulltext : 87259.pdf (Publisher’s version ) (Closed access) We [Hawi et al. (2005); Am J Hum Genet 77:958-965] reported paternal over-transmission of risk alleles in some ADHD-associated genes. This was particularly clear in the case of the DAT1 3'-UTR VNTR. In the current investigation, we analyzed three new sample comprising of 1,248 ADHD nuclear families to examine the allelic over-transmission of DAT1 in ADHD. The IMAGE sample, the largest of the three-replication samples, provides strong support for a parent of origin effect for allele 6 and the 10 repeat allele (intron 8 and 3'-UTR VNTR, respectively) of DAT1. In addition, a similar pattern of over-transmission of paternal ri…

Untranslated region2716 Genetics (clinical)Candidate gene2804 Cellular and Molecular NeuroscienceMedizin610 Medicine & healthMinisatellite RepeatsBiology2738 Psychiatry and Mental HealthGenomic Imprinting03 medical and health sciencesCellular and Molecular Neuroscience0302 clinical medicineSDG 3 - Good Health and Well-beingmental disordersPerception and Action [DCN 1]HumansGenetics(clinical)ddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersRisk factorAllele3' Untranslated RegionsNuclear familyGeneAllelesGenetics (clinical)GeneticsMental Health [NCEBP 9]Dopamine Plasma Membrane Transport ProteinsHaplotypeIntron10058 Department of Child and Adolescent Psychiatry030227 psychiatryPsychiatry and Mental healthHaplotypesAttention Deficit Disorder with Hyperactivity/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being030217 neurology & neurosurgeryAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics
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Methylation status of VTRNA2-1/nc886 is stable across populations, monozygotic twin pairs and in majority of tissues.

2022

Aims & methods: The aim of this study was to characterize the methylation level of a polymorphically imprinted gene, VTRNA2-1/nc886, in human populations and somatic tissues.48 datasets, consisting of more than 30 tissues and >30,000 individuals, were used. Results: nc886 methylation status is associated with twin status and ethnic background, but the variation between populations is limited. Monozygotic twin pairs present concordant methylation, whereas similar to 30% of dizygotic twin pairs present discordant methylation in the nc886 locus. The methylation levels of nc886 are uniform across somatic tissues, except in cerebellum and skeletal muscle. Conclusion: The nc886 imprint may be est…

VTRNA2-1EXPRESSIONCancer Researchpolymorphic imprintingväestötutkimusDISEASEnc886Geneticsnoncoding 886COHORTPLACENTAEXPOSUREgeeniekspressioBRAINEPIGENOME-WIDE ASSOCIATIONRISKDNA methylationgeenit1184 Genetics developmental biology physiologyDna Methylation ; Vtrna2-1 ; Developmental Origins Of Health And Disease Hypothesis ; Imprinting ; Metastable Epiallele ; Nc886 ; Noncoding 886 ; Polymorphic Imprinting ; Population Studiespopulation studies217 Medical engineeringmetastable epialleleDNA-metylaatiodevelopmental origins of health and disease hypothesisHEALTH3111 Biomedicineimprinting
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La naissance des préférences alimentaires

2012

Pourquoi certains enfants adorent les cornichons alors que d’autres détestent le fromage ? Pourquoi sont-ils si attirés vers le sucré ? Pourquoi certains deviennent difficiles à partir de 2 ans ? Quand doit commencer l’éducation alimentaire ? Comment éveiller le goût des enfants et les accompagner vers l’offre de la table familiale ? Quel est le poids des expériences précoces ? Que faire lorsque les courgettes restent dans l’assiette ? Ces questions viennent souvent aux parents des jeunes enfants, qui sont parfois perplexes quant à l’attitude à adopter. Elles sont aussi abordées de manière plus systématique par les chercheurs. Cet exposé montrera quand et comment les préférences alimentaire…

[SDV.AEN] Life Sciences [q-bio]/Food and Nutritionchildrenearly imprinting[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritiondeterminantsfood preference[SDV.AEN]Life Sciences [q-bio]/Food and Nutritioninfantdevelopment
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